Associate II – Complex Generics, Regulatory Affairs (US FDA)
Company: Teva Pharmaceuticals
Location: Bangalore, India
Employment Type: Full-Time
Function: Regulatory Affairs – Complex Generics
Industry: Pharmaceuticals / Generic & Specialty Medicines
Experience Required: 4+ Years
Job ID: 63167
Posting Date: December 11, 2025
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating across nearly 60 countries with a diverse and inclusive workforce. As one of the world’s largest manufacturers of generic medicines and a key contributor to the World Health Organization’s Essential Medicines List, Teva helps more than 200 million patients worldwide access high-quality, affordable healthcare every day.
Role Overview
The Associate II – Complex Generics, Regulatory Affairs is responsible for preparing and submitting high-quality US FDA regulatory filings for complex generic products, including inhalation, ophthalmic, implantable, and drug–device combination products. This role supports both pre-approval and post-approval regulatory activities and requires close collaboration with cross-functional stakeholders to ensure compliance, quality, and on-time submissions.
Working with moderate to minimal supervision, the Associate II manages original applications, amendments, deficiency responses, and post-approval supplements while supporting regulatory strategy execution and process improvement initiatives.
Key Responsibilities
Prepare, review, and compile US FDA regulatory submissions using a right-first-time approach, including:
Original applications
Amendments
Deficiency responses (IRs, DRLs, CRLs)
Support early FDA engagement strategies to align development plans and reduce regulatory risk
Evaluate regulatory impact of change controls, including site transfers, formulation changes, and alternate API sourcing
Determine appropriate post-approval submission pathways (PAS, CBE-30, CBE-0, Annual Reports) in alignment with FDA and internal SOPs
Compile and submit post-approval supplements ensuring compliance with FDA, ICH, and internal regulatory requirements
Serve, as needed, as a regulatory point of contact for cross-functional teams such as R&D, QA, Manufacturing, Packaging, and DMF holders
Monitor and manage regulatory timelines, proactively identifying and resolving data or documentation gaps
Track and interpret updates to FDA regulations and guidance documents relevant to complex generics
Monitor FDA databases (e.g., Drugs@FDA, Orange Book) and communicate relevant regulatory changes internally
Participate in audits, inspections, and continuous process improvement initiatives
Required Experience & Qualifications
Master’s degree in Regulatory Affairs or Quality Assurance, preferably in Pharmaceuticals
Minimum 4+ years of pharmaceutical industry experience, with exposure to:
Inhalation products
Ophthalmic products
Implants
Drug–device combination products
Prior experience in Regulatory Affairs, Analytical, QA, laboratory, or manufacturing environments preferred
Strong understanding of ICH guidelines and US FDA regulatory requirements
Excellent written and verbal communication skills
Strong organizational abilities with attention to detail and effective multitasking skills
Demonstrated critical thinking, problem-solving, and regulatory judgment
Why Join Teva
Work on high-impact, complex generic products regulated by the US FDA
Gain exposure to advanced regulatory pathways and drug–device combination technologies
Collaborate with global, cross-functional teams
Opportunity for long-term career growth in a globally recognized pharmaceutical organization
Inclusive and performance-driven work culture
Equal Employment Opportunity Statement
Teva Pharmaceuticals is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, religion, gender, disability, pregnancy, sexual orientation, gender identity or expression, national origin, or any other legally protected status. Reasonable accommodations are available throughout the recruitment process upon request.
SEO Keywords for Enhanced Visibility
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